HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191816Generated: November 3, 2026
Trifluoroacetic acid → 2-((2-(Dimethylamino)phenyl)amino)-4-phenethylbenzoic acid
https://huagongshe.com/reaction/2191816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoate | HCID 68961327 | — |
| Product | 2-((2-(Dimethylamino)phenyl)amino)-4-phenethylbenzoic acid | HCID 57667958 | — |
Reaction Steps
Trifluoroacetic acid 5.0 mL was added to the obtained tert-butyl 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoate, and it was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure, the obtained residue was refined by reversed-phase silica gel column chromatography [eluent; 50-85% acetonitrile/0.1% trifluoroacetic acid aqueous solution], and ethyl acetate, water and saturated sodium hydrogen carbonate aqueous solution were added to it, and it was adjusted to pH6.5. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. Hexane was added to the obtained residue, and solid matter was filtrated to give 2-((2-(dimethylamino)phenyl)amino)-4-phenethylbenzoic acid 7.0 mg of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08327467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-79807aa4e8b248cebfbcc24c3c976d8b |
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| Source note | uspto-grants-2012_12 |
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